Wiechman B E, Wood T E, Spratto G R
Pharmacol Biochem Behav. 1981 Sep;15(3):425-33. doi: 10.1016/0091-3057(81)90273-2.
The effects of cocaine, procaine, and lidocaine on open field and spontaneous (actophotometer) locomotor activities were assessed and compared in rats (1) treated acutely with morphine (single injection), (2) made dependent on morphine (SC pellets), (3) implanted with morphine and withdrawn at the time of peak dependence, and (4) implanted SC with lactose-containing pellets (sham). Cocaine-induced (10 or 30 mg/kg) open field and spontaneous locomotor activities were significantly greater in each of the four groups than those of the corresponding groups administered saline. Procaine (50 or 100 mg/kg) significantly reduced open field locomotor activity in all morphine-treated rats and spontaneous locomotor activity in acute rats. Lidocaine (30 mg/kg) significantly depressed spontaneous locomotor activity in acute rats. Upon comparison of the activities induced by the three local anesthetics, open field locomotor activity of sham-implanted rats was greater following cocaine (10 or 30 mg/kg) than following procaine (50 or 100 mg/kg). Only morphine withdrawn rats manifested greater activity following cocaine (10 mg/kg) than following either procaine (50 mg/kg) or lidocaine (10 mg/kg); activities were equivalent in dependent and acute rats. In contrast, cocaine-induced (30 mg/kg) open field locomotor activity of all morphine-treated rats was greater than either procaine- (100 mg/kg) or lidocaine- (30 mg/kg) induced activities. Spontaneous locomotor activity of all groups except acute morphine was greater following both doses of cocaine than following both doses of either procaine or lidocaine. In acute rats, only cocaine (10 mg/kg, induced greater activity than the other local anesthetics. Thus, stimulation of locomotor activity following cocaine treatment is a pharmacological property unique to cocaine and not shared by either procaine or lidocaine. Further, the data indicate that the methods selected for assessing locomotor activity may not give comparable results.
评估并比较了可卡因、普鲁卡因和利多卡因对大鼠旷场及自发(活动光度计)运动活动的影响,这些大鼠分为以下四组:(1)急性给予吗啡(单次注射);(2)对吗啡产生依赖(皮下植入药 pellet);(3)植入吗啡并在依赖高峰期撤药;(4)皮下植入含乳糖的药 pellet(假手术组)。可卡因(10或30mg/kg)诱导的旷场及自发运动活动在四组中的每一组均显著高于相应给予生理盐水组。普鲁卡因(50或100mg/kg)显著降低了所有吗啡处理大鼠的旷场运动活动以及急性大鼠的自发运动活动。利多卡因(30mg/kg)显著降低了急性大鼠的自发运动活动。比较三种局部麻醉药诱导的活动时,假手术植入大鼠在给予可卡因(10或30mg/kg)后的旷场运动活动高于给予普鲁卡因(50或100mg/kg)后。只有撤药的吗啡处理大鼠在给予可卡因(10mg/kg)后的活动高于给予普鲁卡因(50mg/kg)或利多卡因(10mg/kg)后的活动;依赖和急性大鼠中的活动相当。相比之下,所有吗啡处理大鼠在给予可卡因(30mg/kg)后的旷场运动活动高于给予普鲁卡因(100mg/kg)或利多卡因(30mg/kg)诱导的活动。除急性吗啡组外,所有组在给予两种剂量的可卡因后的自发运动活动均高于给予两种剂量的普鲁卡因或利多卡因后的活动。在急性大鼠中,只有可卡因(10mg/kg)诱导的活动高于其他局部麻醉药。因此,可卡因处理后对运动活动的刺激是可卡因独有的药理学特性,普鲁卡因和利多卡因均不具备。此外,数据表明选择用于评估运动活动的方法可能无法给出可比的结果。